Heartline Gemini Dissection Forceps 2800-7828L

GUDID 00192896121980

Heartline Gemini Dissection Forceps Spreading Jaw

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00192896121980
NIH Device Record Keyb32629c2-94bf-40bc-9f3e-cac522451cc5
Commercial Distribution StatusIn Commercial Distribution
Brand NameHeartline Gemini Dissection Forceps
Version Model Number2800-7828L
Catalog Number2800-7828L
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Length30.8 Centimeter
Device Size Text, specify0
Length30.8 Centimeter
Device Size Text, specify0
Length30.8 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896121980 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896121980]

Dry Heat Sterilization


[00192896121980]

Dry Heat Sterilization


[00192896121980]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-18
Device Publish Date2025-08-08

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